rs1023835002

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1023835002(A;G)

Make rs1023835002(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

44711547

Gene	B2M, LOC102724979, PATL2

is a	snp
is	mentioned by
dbSNP	rs1023835002
dbSNP (classic)	rs1023835002
ClinGen	rs1023835002
ebi	rs1023835002
HLI	rs1023835002
Exac	rs1023835002
Gnomad	rs1023835002
Varsome	rs1023835002
LitVar	rs1023835002
Map	rs1023835002
PheGenI	rs1023835002
Biobank	rs1023835002
1000 genomes	rs1023835002
hgdp	rs1023835002
ensembl	rs1023835002
geneview	rs1023835002
scholar	rs1023835002
google	rs1023835002
pharmgkb	rs1023835002
gwascentral	rs1023835002
openSNP	rs1023835002
23andMe	rs1023835002
SNPshot	rs1023835002
SNPdbe	rs1023835002
MSV3d	rs1023835002
GWAS Ctlg	rs1023835002

Max Magnitude

0

ClinVar
Risk	rs1023835002(G;G)
Alt	rs1023835002(G;G)
Reference	Rs1023835002(A;A)
Significance	Probable-Pathogenic
Disease	Multiple myeloma Adenocarcinoma of lung Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Colorectal Neoplasms Malignant lymphoma Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the head and neck Small cell lung cancer
Variation	info
Gene	B2M
CLNDBN	Multiple myeloma Adenocarcinoma of lung Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Colorectal Neoplasms Malignant lymphoma, non-Hodgkin Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the head and neck Small cell lung cancer
Reversed	0
HGVS	NC_000015.9:g.45003745A>G; NC_000015.9:g.45003745A>T
CLNSRC
CLNACC	RCV000417544.1, RCV000419609.1, RCV000420829.1, RCV000424715.1, RCV000424903.1, RCV000430542.1, RCV000435632.1, RCV000438049.1, RCV000441263.1, RCV000445210.1, RCV000421861.1, RCV000422880.1, RCV000425118.1, RCV000430300.1, RCV000431428.1, RCV000432545.1, RCV000432685.1, RCV000439880.1, RCV000440097.1, RCV000441906.1,